Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

164968

Sigma-Aldrich

5-Amino-4-imidazolecarboxamide hydrochloride

98%

Synonym(s):

4-Amino-5-imidazolecarboxamide hydrochloride, AICA

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
PLN 100.00
25 G
PLN 209.00

PLN 100.00

Please contact Customer Service for Availability
Request a Bulk Order
All Photos(1)

Select a Size

Change View
5 G
PLN 100.00
25 G
PLN 209.00

About This Item

Empirical Formula (Hill Notation):
C4H6N4O · HCl
CAS Number:
72-40-2
Molecular Weight:
162.58
Beilstein:
3701645
EC Number:
200-778-3
MDL number:
MFCD00012704
UNSPSC Code:
12352005
PubChem Substance ID:
24850109
NACRES:
NA.22
form:
powder
Assay:
98%

PLN 100.00

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

98%

form

powder

mp

250-252 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, clear, light yellow

functional group

amide

SMILES string

Cl[H].NC(=O)c1[nH]cnc1N

InChI

1S/C4H6N4O.ClH/c5-3-2(4(6)9)7-1-8-3;/h1H,5H2,(H2,6,9)(H,7,8);1H

InChI key

MXCUYSMIELHIQL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Corrosion inhibition and adsorption characteristics of 5-amino-4-imidazolecarboxamide hydrochloride on aluminum in 1M HCl has been investigated[1].

Application

5-Amino-4-imidazolecarboxamide hydrochloride was used in the synthesis of heterocyclic compounds such as guanine[2], purines[3][4] and pyrimidines[5].

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBL3808
SDBB0597
S04888
S40246
04820PT

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The Journal of Organic Chemistry, 56, 2139-2139 (1991)
Fang Li et al.
Scientific reports, 6, 37114-37114 (2016-11-22)
GRS is a drug combination of three active components including ginsenoside Rb1, ruscogenin and schisandrin. It derived from the well-known TCM formula ShengMai preparations, a widely used traditional Chinese medicine for the treatment of cardiovascular diseases in clinic. The present
Heterocycles, 34, 1133-1133 (1992)
Journal of Heterocyclic Chemistry, 30, 593-593 (1993)
Brandon Tran et al.
Cell chemical biology, 27(10), 1241-1249 (2020-08-17)
Riboswitches are mRNA domains that make gene-regulatory decisions upon binding their cognate ligands. Bacterial riboswitches that specifically recognize 5-aminoimidazole-4-carboxamide riboside 5'-monophosphate (ZMP) and 5'-triphosphate (ZTP) regulate genes involved in folate and purine metabolism. Now, we have developed synthetic ligands targeting
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service